The quality of evidence is downgraded by study limitations (unclear allocation concealment and selective outcome reporting).
A Cochrane review included 50 studies with a total of 27 139 subjects; 44 studies (n=21 460) compared an antiplatelet agent with placebo or no treatment, and 6 studies (n=5 679) directly compared one antiplatelet agent with another. Compared to placebo or no treatment, antiplatelet agents reduced the risk of myocardial infarction (RR 0.87, 95% CI 0.76 to 0.99; 17 studies), but not all-cause mortality (RR 0.93, 95% CI 0.81 to 1.06; 30 studies), cardiovascular mortality (RR 0.89, 95% CI 0.70 to 1.12; 19 studies) or stroke (RR 1.00, 95% CI 0.58 to 1.72; 11 studies). Antiplatelet agents increased the risk of major (RR 1.33, 95% CI 1.10 to 1.65; 27 studies) and minor bleeding (RR 1.49, 95% CI 1.12 to 1.97; 18 studies). In terms of dialysis access outcomes, antiplatelet agents reduced access thrombosis or patency failure but had no effect on suitability for dialysis. Limited data were available for direct head-to-head comparisons of antiplatelet drugs, treatment in kidney transplant recipients, primary prevention, or risk of end-stage kidney disease.
Risks may outweigh benefits among people with low annual risks of cardiovascular events, including those with early stages of chronic kidney disease who do not have clinically-evident occlusive cardiovascular disease.
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